RateMyPlacement
My role involved connecting with key internal stakeholders in order to understand about different patient engagement projects happening across the business. I also attended various meetings with external stakeholders and agencies and autonomously worked on various projects I was leading on.
Daily tasks - tracking regulatory submissions, preparing documents to submit to regulators, responding to queries about submissions from regulators Daily interactions - liaise with regulatory colleagues to make strategic decisions on products licensure in various regions, liaise with labelling colleagues to ensure the relevant updates are made to a product's labelling, liaise with submissions management to plan and carry out regulatory submissions Responsibilities - maintaining licences (renewals, PSURs), marketing authorisation applications, CTA amendments, variations
No day was the same for me. My manager truly tailored the role to my goals and aspirations and it kept moving from one project to another. Below are some of the activities that I engaged with throughout my placement. Analysed voluminous data to create a monthly metrics report, entailing performance insights on marketing channels for regular senior leadership team reviews. Delivered high-value email-campaigns under tight deadlines whilst working with cross-functional teams such as my alliance partners, creative agencies, medical team and other external stakeholders. Used A/B testing to select an optimal marketing channel mix for providing national visibility to sales representative led meetings, thus exceeding local benchmarks by 220%. Designed a brand website by learning new software tools and implementing an engaging UX journey whilst delivering this global project within 20 days. Led on a project to increase Pfizer sign-ups to company's email newsletters and embedded track links for effective mapping of success KPIs. Successfully contributed to closing the Gender Pay Gap by 5% through brainstorming on ideas and implementing them with the Diversity and Inclusion team.
Overseeing and managing the execution of clinical trials by working closely with a global team of other study members that have different roles within the company. You get to shadow a study manager and learn from them. During the placement year you also get to also work with other undergraduates and are led by a manager who is there to support you and guide you during your stay at Pfizer.
1) I check my emails as Pfizer is a global company, things often come in overnight. 2) I will have meetings for various projects throughout the day, often planned but urgent ones for new tasks aren't uncommon. 3) complete paperwork for different submission's or queries including sending emails across the company to get documents or information required. 4) partake in social activities with undergrads. Each day is different as workflow varies a lot
Managing and identifying projects that will improve the reliability and sustainability of building services on the site. This involves liaising with contracted parties from various disciplines. The role also has a focus on energy management and analysis, which is used to detect overspends and identify energy saving opportunities.
My work involves maintaining the internal communication between markets, developing materials, organizing global events, managing logistics, and leading sponsorships.
I work on innovative projects aiming to automate parts of the publishing process to reduce overall costs to the business. Day-to-day, I will monitor the progress of any projects I am currently working on, provide updates to the EU team on the progress of these projects, coordinate the EU Publishing team's efforts on particular Pfizer products, meetings with colleagues across all of our sites globally, answering queries from colleagues relating to the projects I am working on etc.
Acquisition and in-depth analysis of forensic evidence collected from a range of devices and operating systems ● Daily use of industry standard digital forensic tools such as: ○ Encase Investigator ○ Nuix Workstation and Investigate (Formerly Web Review) ○ Magnet Forensics Axiom ○ FTK Imager ○ BlackLight ○ Autopsy ● Communicated with customers to explain and update on forensic investigations ● Authored forensic reports to provide detailed technical break-downs of our investigations
Answering queries relating to the GPG and its workstreams, creating resources for people to use to help progress their career, attending/running and helping to create workshops for employees around flexible working and career progression. As well as creating data to inform metrics about how they are working.
I have worked closely with the marketing team to implement key strategies and tactics as well as contribute to future strategic directions. I have managed materials from development to approval and dissemination which has been great to see how projects run from start to finish. I have also worked closely with agencies and other external stakeholders. I managed the orders and stock of materials. Day-to-day activities vary but I was always kept busy with a range of projects and meetings.
Support the study team on multiple phase 1-4 vaccine trials. Attend meetings, review documents, prepare presentations, keep up with larger projects.
Preparing promotional materials to support our key messaging.
Working with the anti-infectives marketing team, as well as external stakeholders such as creative agencies, to support with the development and approval of materials in line with key brand initiatives. Day to day role would involve 2-3 meetings (e.g. status calls for projects, catch-up with team, training sessions), replying to and sending emails about various projects and otherwise working independently to deliver projects on time.
I have worked both in the development and post-approval space on a range of products. The main task has been supporting regulatory submissions. On a day to day basis this has involved participating in team meetings and working autonomously as well as part of a larger team.
Been involved on a Marketing Authorisation Application and given lead roles within this. Been given the opportunity to branch into other departments. General daily activities including checking emails and replying to colleagues, however often each day is different and brings new things to do and new projects to get involved in. Lots of coordinating between people involved, in order to make sure everything is submitted on time.
I worked on 3 different projects in my time at Pfizer. Two of them were data science roles and the other one was HPLC based. Daily tasks would involve things such as data processing, communicating progress to project leaders, organising meetings where necessary, responding to relevant emails. Weekly check in meetings would occur with my manager and some projects also have their own meetings, e.g every six weeks to catch up with everyone involved in that team.
Key responsibilities included the development of promotional and non-promotional marketing materials, project management, liaising with external creative agencies, increasing customer engagement through third-party channels, congress management, budget management.
Laboratory based role, use a variety of analytical techniques such as LC-MS and NMR. Development of analytical methods and technologies, research into new ways to implement them. Analysis of data conducted independently and written up coherently
My role was based within the Article 57 team in Global Regulatory Operations. This consisted of 'Business as Usual' work within the team, alongside project based work for a wider audience throughout Pfizer
